Issue 32, 2017, Issue in Progress

The relative length of dual-target conjugated on iron oxide nanoparticles plays a role in brain glioma targeting

Abstract

The application of superparamagnetic iron oxide nanoparticles as a magnetic resonance (MR) nanoprobe for brain glioma is limited by the insufficient specificity and accumulation at the tumor site. To increase brain glioma-targeting specificity and improve MR contrast effect, dual-target has been employed. However, up to now, little work has been done to ascertain if the relative length of the dual-target plays a role in targeting. Herein, we prepared Cy5.5-labeled Fe3O4 NPs with chlorotoxin (CTX)/PEGylated folic acid (PEG-FA) dual-target of different relative lengths. The effect of dual-target relative length on targeting specificity was investigated by in vitro cellular uptake and in vivo MR/NIR imaging in brain glioma-bearing mice. It was demonstrated that the targeting ability of the dual-targeting Fe3O4 NPs could be modulated by adjusting the relative length of dual-target, suggesting that the relative length of dual-target plays a role in brain glioma targeting.

Graphical abstract: The relative length of dual-target conjugated on iron oxide nanoparticles plays a role in brain glioma targeting

Supplementary files

Article information

Article type
Paper
Submitted
20 Feb 2017
Accepted
29 Mar 2017
First published
05 Apr 2017
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2017,7, 19954-19959

The relative length of dual-target conjugated on iron oxide nanoparticles plays a role in brain glioma targeting

P. Ai, H. Wang, K. Liu, T. Wang, W. Gu, L. Ye and C. Yan, RSC Adv., 2017, 7, 19954 DOI: 10.1039/C7RA02102J

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